Congenitally uncorrected transposition of the great arteries
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Congenitally uncorrected transposition of the great vessels Ventriculoarterial discordance with atrioventricular concordance Isolated ventriculoarterial discordance |
| Number of Symptoms | 1 |
| OrphanetNr: | 860 |
| OMIM Id: |
608808
613853 613854 |
| ICD-10: |
Q20.3 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Multifactorial Not applicable [Orphanet] |
| Age of onset: |
Neonatal Infancy [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic cardiac anomaly
-Rare genetic disease Transposition of the great arteries -Rare developmental defect during embryogenesis |
Symptom Information:
|
|
(HPO:0001669) | Transposition of the great arteries | 36 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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